Canonical Allele Identifier: PA2580510272
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2097428
ClinVar RCV Id: RCV003016696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Gly13Cys
CA402998401
NM_138924.3:c.37G>T